Bioresorbable Nonwoven Patches as Taxane Delivery Systems for Prostate Cancer Treatment

Joanna Jaworska1, Arkadiusz Orchel2, Anna Kaps2

  • 1Centre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 34, 41-819 Zabrze, Poland.

Pharmaceutics
|December 23, 2022
PubMed

Insights

Drug-eluting bioresorbable patches loaded with Cabazitaxel (CTX) show promise for treating prostate cancer. These patches effectively reduce cancer cell growth locally after surgery, offering a potential new therapy.

Area of Science:

  • Biomaterials Science
  • Oncology
  • Drug Delivery Systems

Background:

  • Prostate cancer is a leading cancer in males, often treated with radical prostatectomy.
  • Recurrence post-surgery is a significant clinical challenge.
  • Local drug delivery systems could reduce recurrence risk at tumor sites or resection margins.

Purpose of the Study:

  • To develop and evaluate drug-eluting bioresorbable electrospun patches for local delivery of chemotherapy agents.
  • To assess the drug release profile, anticancer activity, and biocompatibility of these patches for prostate cancer therapy.

Main Methods:

  • Electrospinning was used to create drug-loaded patches using polyesters and polyestercarbonates.
  • Patches loaded with Cabazitaxel (CTX) or Docetaxel (DTX) were fabricated.
  • In vitro drug release, cytotoxicity assays using PC-3 and DU145 cells, and biocompatibility tests were performed.

Main Results:

  • Cabazitaxel (CTX)-loaded patches demonstrated sustained drug release over three months (60% release).
  • CTX-loaded patches significantly reduced prostate cancer cell growth (53% for PC-3, 31% for DU145) compared to controls.
  • Drug-free patches exhibited excellent biocompatibility with the PC-3 cell line.

Conclusions:

  • Cabazitaxel-loaded bioresorbable electrospun patches represent a promising local drug delivery system for prostate cancer.
  • This approach has therapeutic potential for reducing post-surgical recurrence.
  • The developed patches show good biocompatibility and efficacy in preclinical models.